(Q28204157)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

main subject

rippling muscle disease

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Alfredo Ramirez

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Valentin Stein

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Markus M Nöthen

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

André Reis

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Thomas Jentsch

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Christian Kubisch

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

Betz RC

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Kasper D

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Ricker K

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Torbergsen T

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Lee YA

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Wienker TF

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Malin JP

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Propping P

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Mortier W

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Vorgerd M

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

language of work or name

English

0 references

publication date

1 July 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

218-219

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11431690%20AND%20SRC:MED&resulttype=core&format=json

A family with dominant hereditary myotonia, muscular hypertrophy, and increased muscular irritability, distinct from myotonia congenita thomsen

9 November 2019

cites work

1 reference

7 January 2021

Rippling muscle disease

1 reference

7 January 2021

A rippling muscle disease gene is localized to 1q41: evidence for multiple genes

1 reference

7 January 2021

Phenotypic variability in rippling muscle disease

1 reference

7 January 2021

Molecular cloning of caveolin-3, a novel member of the caveolin gene family expressed predominantly in muscle

1 reference

7 January 2021

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

1 reference

7 January 2021

Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy

1 reference

7 January 2021

Mutation in the CAV3 gene causes partial caveolin-3 deficiency and persistent elevated levels of serum creatine kinase

1 reference

7 January 2021

Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex

1 reference

7 January 2021

Nitric oxide synthases: which, where, how, and why?

1 reference

7 January 2021

Physiology of nitric oxide in skeletal muscle

1 reference

7 January 2021

Caveolin-3 deficiency causes muscle degeneration in mice

1 reference

7 January 2021

Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity

1 reference

7 January 2021